List of works - Bergithe E Oftedal

21-hydroxylase and interferon omega autoantibodies in Turner syndrome

21-hydroxylase autoantibodies are more prevalent in Turner syndrome but without an association to the autoimmune polyendocrine syndrome type I

scientific article published on 14 November 2018

8q13.1-q13.2 deletion associated with inferior cerebellar vermian hypoplasia and digital anomalies: a new syndrome?

scientific article published on 13 October 2014

A Longitudinal Follow-up of Autoimmune Polyendocrine Syndrome Type 1.

scientific article published on 02 June 2016

A Variant in the BACH2 Gene Is Associated With Susceptibility to Autoimmune Addison's Disease in Humans

scientific article published on 28 September 2016

AIRE variations in Addison's disease and autoimmune polyendocrine syndromes (APS): partial gene deletions contribute to APS I

article

AIRE-mutations and autoimmune disease

scientific article

ARMC5 mutations are common in familial bilateral macronodular adrenal hyperplasia

scientific article published on 06 June 2014

Altered Immune Activation and IL-23 Signaling in Response to Candida albicans in Autoimmune Polyendocrine Syndrome Type 1

scientific article

Anti-cytokine autoantibodies preceding onset of autoimmune polyendocrine syndrome type I features in early childhood.

scientific article published on 26 October 2013

Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease

scientific article published on 27 September 2019

Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases

scientific journal article

Expanding the Phenotypic and Genotypic Landscape of Autoimmune Polyendocrine Syndrome Type 1.

scientific article

Flow cytometry study of blood cell subtypes reflects autoimmune and inflammatory processes in autoimmune polyendocrine syndrome type I.

scientific article

GWAS for autoimmune Addison's disease identifies multiple risk loci and highlights AIRE in disease susceptibility

scientific article published on 11 February 2021

Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease

scientific article published on 01 April 2019

Impaired salivary gland activity in patients with autoimmune polyendocrine syndrome type I.

scientific article

Ligand-dependent protein interactions of the estrogen receptors using the yeast two-hybrid system

scientific article published on April 2005

Measuring Autoantibodies against IL-17F and IL-22 in Autoimmune Polyendocrine Syndrome Type I by Radioligand Binding Assay Using Fusion Proteins

scientific article published on 7 August 2011

New ERA of therapy for endocrine autoimmune disorders

scientific article published on 27 August 2020

Oral microbiota in autoimmune polyendocrine syndrome type 1.

scientific article published on 26 February 2018

Radioimmunoassay for autoantibodies against interferon omega; its use in the diagnosis of autoimmune polyendocrine syndrome type I

scientific article published in October 2008

Radioligand-binding assay reveals distinct autoantibody preferences for type I interferons in APS I and myasthenia gravis subgroups

scientific article published on 30 November 2011

Revealing Missing Human Protein Isoforms Based on Ab Initio Prediction, RNA-seq and Proteomics

scientific article published on 9 July 2015

T cell receptor assessment in autoimmune disease requires access to the most adjacent immunologically active organ.

scientific article published on 15 March 2017

The chaperonin CCT8 controls proteostasis essential for T cell maturation, selection, and function

scientific article published on 03 June 2021

The prospects of single-cell analysis in autoimmunity

scientific article published on 01 September 2020

Transcriptional Changes in Regulatory T Cells From Patients With Autoimmune Polyendocrine Syndrome Type 1 Suggest Functional Impairment of Lipid Metabolism and Gut Homing

scientific article published on 30 August 2021

List of works by Bergithe E Oftedal

21-hydroxylase and interferon omega autoantibodies in Turner syndrome

21-hydroxylase autoantibodies are more prevalent in Turner syndrome but without an association to the autoimmune polyendocrine syndrome type I

8q13.1-q13.2 deletion associated with inferior cerebellar vermian hypoplasia and digital anomalies: a new syndrome?

A Longitudinal Follow-up of Autoimmune Polyendocrine Syndrome Type 1.

A Variant in the BACH2 Gene Is Associated With Susceptibility to Autoimmune Addison's Disease in Humans

AIRE variations in Addison's disease and autoimmune polyendocrine syndromes (APS): partial gene deletions contribute to APS I

AIRE-mutations and autoimmune disease

ARMC5 mutations are common in familial bilateral macronodular adrenal hyperplasia

Altered Immune Activation and IL-23 Signaling in Response to Candida albicans in Autoimmune Polyendocrine Syndrome Type 1

Anti-cytokine autoantibodies preceding onset of autoimmune polyendocrine syndrome type I features in early childhood.

Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease

Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases

Expanding the Phenotypic and Genotypic Landscape of Autoimmune Polyendocrine Syndrome Type 1.

Flow cytometry study of blood cell subtypes reflects autoimmune and inflammatory processes in autoimmune polyendocrine syndrome type I.

GWAS for autoimmune Addison's disease identifies multiple risk loci and highlights AIRE in disease susceptibility

Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease

Impaired salivary gland activity in patients with autoimmune polyendocrine syndrome type I.

Ligand-dependent protein interactions of the estrogen receptors using the yeast two-hybrid system

Measuring Autoantibodies against IL-17F and IL-22 in Autoimmune Polyendocrine Syndrome Type I by Radioligand Binding Assay Using Fusion Proteins

New ERA of therapy for endocrine autoimmune disorders

Oral microbiota in autoimmune polyendocrine syndrome type 1.

Radioimmunoassay for autoantibodies against interferon omega; its use in the diagnosis of autoimmune polyendocrine syndrome type I

Radioligand-binding assay reveals distinct autoantibody preferences for type I interferons in APS I and myasthenia gravis subgroups

Revealing Missing Human Protein Isoforms Based on Ab Initio Prediction, RNA-seq and Proteomics

T cell receptor assessment in autoimmune disease requires access to the most adjacent immunologically active organ.

The chaperonin CCT8 controls proteostasis essential for T cell maturation, selection, and function

The prospects of single-cell analysis in autoimmunity

Transcriptional Changes in Regulatory T Cells From Patients With Autoimmune Polyendocrine Syndrome Type 1 Suggest Functional Impairment of Lipid Metabolism and Gut Homing